Active participation in method development, validation and subject sample analysis.
Process and analyze the subject samples as per the project requirements.
Managing the regulatory aspects of projects and products for pre-approval and post approval submissions for biological, new drugs and global and local clinical trials. In addition, participating in project team meetings, by providing regulatory support to ensure compliance with all local requirements.
5 years research, teaching and design and development experience after M.VSc, M.Pharma, ME, M.Tech, M.Sc Life science, Biotechnology. One research paper in Science Citation indexed Journal is Desirable.
To clone, sub-clone, design mutants, express and purify proteins. Perform biochemical, biophysical and structural biology studies with relevant proteins to characterize their interactions.
The incumbent should be experienced with the product development flow from the conceptualization to tech transfer. The incumbent is responsible for R&D trails batch making for various person care & food products like
Encube Ethicals is a pharmaceutical company dedicated to only topical formulations serving patients and leading pharmaceutical brands around the world. with high-quality, affordable topical products.
Encube Ethicals are hiring for Analytical Transdermal department
Masters in Life Sciences. Participate, as needed, on global teams to complete assignments and tasks within a specific task force/project associated with labelling